Canonical Allele Identifier: CA237623592
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs973781099
gnomAD v2: 12-56435666-G-C
gnomAD v3: 12-56041882-G-C
gnomAD v4: 12-56041882-G-C
MyVariant Identifiers: chr12:g.56435666G>C (hg19) chr12:g.56041882G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041882G>C , CM000674.2:g.56041882G>C GRCh38
NC_000012.11:g.56435666G>C , CM000674.1:g.56435666G>C GRCh37
NC_000012.10:g.54721933G>C NCBI36
NG_023201.1:g.4981G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-285G>C ENSP00000348849.5:n.-285G>C
ENST00000356464.9:c.-285G>C ENSP00000348849.5:n.-285G>C
XR_944989.3:n.122C>G
XR_944990.3:n.122C>G
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